EZ2go Stimu-Lax by Valley Medical Products, LLC / LNK International, Inc.

EZ2go Stimu-Lax by

Drug Labeling and Warnings

EZ2go Stimu-Lax by is a Otc medication manufactured, distributed, or labeled by Valley Medical Products, LLC, LNK International, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

EZ2GO STIMU-LAX- bisacodyl tablet 
Valley Medical Products, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Active Ingredients

Drug Facts

Active Ingredients (in each tablet)

Bisacodyl USP, 5 mg

Purpose

Purpose

Stimulant laxative

Keep Out Of Reach Of Children

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Uses

Uses

  • For temporary relief of occasional constipation and irregularity
  • Generally produces a bowel movement in 6 to 12 hours

Warnings

Warnings

Do not use : if you cannot swallow without chewing.

When using this product

  • Do not chew or crush tablet(s)
  • Do not use within 1 hour after taking an antacid or milk
  • it may cause stomach discomfort, faintness and cramps

Ask A Doctor Before Use If You Have Stop Use And Ask Doctor If

Ask a doctor before use if you have

  • Stomach pain, nausea or vomiting
  • A sudden change in bowel habits that lasts more than 2 weeks

Stop use and ask a doctor if

  • You have rectal bleeding or no bowel movement after using this product. These could be signs of a serious condition.
  • If you need to use a laxative for more than 1 week

If Pregnant Or Breast-Feeding

If pregnant or breast-feeding, ask a health professional before use.

Directions

Directions

  • Take with a glass of water

Adults and children 12 years of age and older; 1-3 tablets in a single daily dose

Children 6 to under 12 years of age; 1 tablet in a single daily dose

Children under 6 tears of age; ask a doctor

Other Information

Other information:

  • Store at 20-25 degrees C (68-77 degrees F)
  • Protect from excessive humidity
  • Packaged for your protection.

Do not use if individual seals are broken.

Inactive Ingredients

Inactive ingredients

Calcium Carbonate, Dicalcium Phosphate, Cellulose, Stearic Acid, Maltodextrin, Croscarmellose Sodium, Pharmaceutical Glaze, Magnesium Stearate, Silicon Dioxide, Carnauba Wax.

Questions Or Comments

Questions or comments?

800-403-9832 or wwwez2go.com

Package Label

NDC: 76470-004-04

EZ2go Stimu-Lax

  • Laxative
  • Bisacodyl

1 DOSE 5 mg tablet

  • Doctor Recommended
  • Easily Dissolvable
  • Stool Softener
  • Controls Irregularity

NSF  Live safer.

Maunfactured for, Copyright and Distributed by Valley Medical Products, LLC, Ponte Vedra Beach, FL 32082 USA  All rights

www.ex2go.com or call 800-403-9832

Valley MP EZ2goStimu-Lax Label


EZ2GO STIMU-LAX 
bisacodyl tablet
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 76470-004
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
BISACODYL (UNII: 10X0709Y6I) (DEACETYLBISACODYL - UNII:R09078E41Y) BISACODYL5 mg  in 5 mg
Inactive Ingredients
Ingredient NameStrength
CALCIUM CARBONATE (UNII: H0G9379FGK)  
CALCIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: L11K75P92J)  
POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
MALTODEXTRIN (UNII: 7CVR7L4A2D)  
CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
SHELLAC (UNII: 46N107B71O)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
CARNAUBA WAX (UNII: R12CBM0EIZ)  
Product Characteristics
Colorwhite (WHITE) Scoreno score
ShapeROUND (TABLET) Size4mm
FlavorImprint Code VMP
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 76470-004-002 in 1 BOX04/01/201211/30/2014
1NDC: 76470-004-045 mg in 1 POUCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33404/01/201211/30/2014
Labeler - Valley Medical Products, LLC (969389407)
Registrant - Valley Medical Products, LLC (969389407)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.038154464pack(76470-004)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867837pack(76470-004)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.832867894manufacture(76470-004)
Establishment
NameAddressID/FEIBusiness Operations
LNK International, Inc.967626305pack(76470-004)

Revised: 7/2019
 
Valley Medical Products, LLC